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CHMP1A Gene Pontocerebellar Hypoplasia Type 8 Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The CHMP1A gene pontocerebellar hypoplasia type 8 genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the CHMP1A gene that are associated with pontocerebellar hypoplasia type 8 (PCH8). This condition is a rare genetic disorder characterized by the underdevelopment of the cerebellum and brainstem, leading to significant neurological impairments. The test is crucial for early diagnosis, which can aid in the management and treatment planning for affected individuals. The cost of the test is set at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic mutation. This test is an essential tool for families with a history of PCH8, providing them with valuable information regarding their genetic health and the risk of passing the condition to future generations.

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CHMP1A Gene Pontocerebellar Hypoplasia Type 8 Genetic Test

Welcome to DNA Labs UAE, where we offer the CHMP1A Gene Pontocerebellar Hypoplasia Type 8 Genetic Test. This test is designed to diagnose and provide information about the rare neurodevelopmental disorder known as pontocerebellar hypoplasia type 8 (PCH8).

Test Components

  • Test Name: CHMP1A Gene Pontocerebellar Hypoplasia Type 8 Genetic Test
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the CHMP1A Gene Pontocerebellar Hypoplasia Type 8 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with CHMP1A Gene Pontocerebellar Hypoplasia Type 8.

Test Details

The CHMP1A gene is associated with pontocerebellar hypoplasia type 8 (PCH8), a rare neurodevelopmental disorder characterized by underdevelopment of the pons and cerebellum. This condition leads to various neurological symptoms. Our NGS (Next-Generation Sequencing) genetic testing method allows for the simultaneous analysis of multiple genes to identify variations or mutations in the DNA sequence. Specifically for PCH8, the NGS genetic testing can identify mutations or variations in the CHMP1A gene that may be responsible for the condition. This analysis of the CHMP1A gene’s DNA sequence helps in diagnosing PCH8, providing information about the specific genetic variant involved, and assisting in genetic counseling and family planning.

It is crucial to consult with a healthcare professional or a genetic counselor to discuss the benefits, limitations, and potential implications of the CHMP1A Gene Pontocerebellar Hypoplasia Type 8 Genetic Test.

Test Name CHMP1A Gene Pontocerebellar hypoplasia type 8 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for CHMP1A Gene Pontocerebellar hypoplasia type 8 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CHMP1A Gene Pontocerebellar hypoplasia type 8
Test Details

The CHMP1A gene is associated with a genetic condition called pontocerebellar hypoplasia type 8 (PCH8). PCH8 is a rare neurodevelopmental disorder characterized by underdevelopment (hypoplasia) of the pons and cerebellum, leading to various neurological symptoms.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify variations or mutations in the DNA sequence. In the case of PCH8, NGS genetic testing can be used to identify mutations or variations in the CHMP1A gene that may be responsible for the condition.

By analyzing the DNA sequence of the CHMP1A gene, NGS testing can help diagnose PCH8, provide information about the specific genetic variant involved, and assist in genetic counseling and family planning.

It’s important to consult with a healthcare professional or a genetic counselor to discuss the specifics of the test, including its benefits, limitations, and potential implications.

SKU: TEST-1931 Category:

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